Your data on MRCVSonline
The nature of the services provided by Vision Media means that we might obtain certain information about you.
Please read our Data Protection and Privacy Policy for details.

In addition, (with your consent) some parts of our website may store a 'cookie' in your browser for the purposes of
functionality or performance monitoring.
Click here to manage your settings.
If you would like to forward this story on to a friend, simply fill in the form below and click send.

Your friend's email:
Your email:
Your name:
 
 
Send Cancel

WHO approves fast test for Ebola
blood test
Trials of the test have correctly identified around 92 per cent of patients who have been infected with the virus.
Test provides results in 15 minutes

A blood test for Ebola which can provide results within 15 minutes has been approved for use by the World Health Organisation.

According to the BBC, the test will allow patients to be identified, isolated and cared for as quickly as possible in an attempt to tackle the outbreak, which has now killed over 9,000 people.

Ebola is currently being tested in laboratories largely through the detection of the virus's nucleic acid, using commercial or in-house tests.

Nucleic acid tests (NATs) are more accurate but are complex to use and require well-established laboratories and fully trained personnel. The turn-around time for a NAT test is also quite slow, varying between 12 and 24 hours.

WHO say that the ReEBOV Antigen Rapid Test, developed by US company Corgenix,  is based on detection of the Ebola protein rather that nucleic acid.

Trials of the test have correctly identified around 92 per cent of patients who have been infected with the virus.

The World Health Organisation said: "While less accurate, the antigen test is rapid, easy to perform and does not require electricity – it can therefore be used at lower health care facilities or in mobile units for patients in remote settings"

It added that where possible, results from ReEBOV antigen Rapid Test Kit should be confirmed by testing a new blood sample using an approved Ebola NAT.

Become a member or log in to add this story to your CPD history

Defra shares new Sanitary and Phytosanitary guidance

News Story 1
 Defra has published guidance for the vet sector ahead of a proposed UK-EU Sanitary and Phytosanitary agreement.

The agreement, which will change the movement and trade of animals and related products, could see reductions in checks, paperwork and certification. As well as describing regulatory developments, the advice highlights the importance of animal ID, registration and traceability in disease control and other compliance arrangements.

The guidance can be found here. More detail is expected as negotiations progress. 

Click here for more...
News Shorts
New form for online veterinary medicines retailers

The Veterinary Medicines Directorate (VMD) has produced a new online form for retailers wishing to sell veterinary medicines on the internet.

The form replace the previous Word version and is part of the VMD's ongoing commitment to digitise its processes. Anyone retailing prescription medicines online, including POM-V, POM-VPS and NFA-VPS categories, is lawfully required to register with the VMD before trading.

The change only applies to new applicants. Retailers already listed on the VMD's Register of Online Retailers or registered under the Accredited Internet Retailer Scheme (AIRS) do not need to do anything.